US20160054228A1 - Total nitrogen measurement apparatus - Google Patents
Total nitrogen measurement apparatus Download PDFInfo
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- US20160054228A1 US20160054228A1 US14/378,694 US201214378694A US2016054228A1 US 20160054228 A1 US20160054228 A1 US 20160054228A1 US 201214378694 A US201214378694 A US 201214378694A US 2016054228 A1 US2016054228 A1 US 2016054228A1
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- United States
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- light emission
- sample water
- measurement
- total nitrogen
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 title claims abstract description 66
- 238000005259 measurement Methods 0.000 title claims abstract description 39
- 229910052757 nitrogen Inorganic materials 0.000 title claims abstract description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 40
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 35
- 229910052742 iron Inorganic materials 0.000 claims abstract description 20
- -1 nitrate ions Chemical class 0.000 claims abstract description 20
- 229910017464 nitrogen compound Inorganic materials 0.000 claims abstract description 17
- 150000002830 nitrogen compounds Chemical class 0.000 claims abstract description 17
- 238000006243 chemical reaction Methods 0.000 claims abstract description 16
- 229910002651 NO3 Inorganic materials 0.000 claims abstract description 14
- 239000000463 material Substances 0.000 claims abstract description 12
- 238000006864 oxidative decomposition reaction Methods 0.000 claims abstract description 12
- 238000011481 absorbance measurement Methods 0.000 claims abstract description 5
- 229920005989 resin Polymers 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims description 2
- 238000007254 oxidation reaction Methods 0.000 description 22
- 230000003647 oxidation Effects 0.000 description 20
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 229920002050 silicone resin Polymers 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
- 238000002835 absorbance Methods 0.000 description 6
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical group O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- 238000001514 detection method Methods 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical class [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 239000012070 reactive reagent Substances 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 229920002449 FKM Polymers 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920006333 epoxy cement Polymers 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000010842 industrial wastewater Substances 0.000 description 1
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- VLAPMBHFAWRUQP-UHFFFAOYSA-L molybdic acid Chemical compound O[Mo](O)(=O)=O VLAPMBHFAWRUQP-UHFFFAOYSA-L 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000002798 spectrophotometry method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/18—Water
- G01N33/188—Determining the state of nitrification
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
- G01N21/33—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using ultraviolet light
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/631—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited using photolysis and investigating photolysed fragments
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N31/00—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
- G01N31/005—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods investigating the presence of an element by oxidation
Definitions
- the present invention relates to a total nitrogen measurement apparatus including a reaction vessel having a space where a light emission section of an ultraviolet lamp is to be inserted and where a sample is to be contained in a space around the ultraviolet lamp, the total nitrogen measurement apparatus being for measuring the concentration of nitrogen compounds in a sample by decomposing nitrogen compounds by oxidation by holding, in the reaction vessel, a sample water to which a reactive reagent is added to perform oxidative decomposition of nitrogen compounds and radiating ultraviolet rays from the ultraviolet lamp on the sample water, and performing absorbance measurement on the sample water obtained after the nitrogen compounds have been decomposed by oxidation.
- total nitrogen concentration is determined by decomposing nitrogen compounds in a sample water to which alkaline potassium peroxodisulfate, which is an oxidizing agent, is added into nitrate ions by oxidation by radiating ultraviolet rays on the sample water under a condition of predetermined temperature and pressure, and measuring the absorbance of the sample water at 220 nm.
- This method is improved in reducing the pressure and temperature for the sample water, and the temperature necessary for oxidative decomposition of nitrogen oxide by ultraviolet rays is reduced to about 60° C. from conventional 120° C., and also, the pressure may be a normal pressure, and thus, the apparatus is not required to be highly resistant to pressure and heat.
- Patent Document 1 Japanese Patent Laid-open Publication No. 2003-344381
- a detection signal obtained by performing total nitrogen measurement by an apparatus adopting such a structure sometimes includes a signal which is thought to be caused by the influence of a substance different from the nitrate ions generated by oxidative decomposition of the nitrogen compounds, and the cause of the obtained detection signal is yet to be explained.
- the present invention aims to prevent, in measurement of absorbance of a sample water including nitrate ions which have been converted by ultraviolet radiation, interference in total nitrogen measurement by substances other than the nitrate ions.
- the present invention is a total nitrogen measurement apparatus including a reaction vessel having a space where a light emission section of an ultraviolet lamp is to be inserted and where a sample is to be contained in a space around the ultraviolet lamp, the total nitrogen measurement apparatus being for measuring a total nitrogen concentration of a sample water by converting nitrogen compounds into nitrate ions by oxidative decomposition by holding, in the reaction vessel, a sample to which a reactive reagent is added to perform oxidative decomposition of the nitrogen compounds and radiating ultraviolet rays from the ultraviolet lamp on the sample water, and performing absorbance measurement on the sample water including the nitrate ions, wherein a holding section for holding the light emission section of the ultraviolet lamp is formed of a material not including iron.
- the cause of the noise is the ultraviolet lamp which is for radiating ultraviolet rays on the sample water to decompose the nitrogen compounds by oxidation. That is, although the only part of the ultraviolet lamp that comes into contact with a sample water is a light emission section formed of a material not including iron-based material, such as a quartz glass tube, an external cylinder portion of a holding section for holding the base portion of the light emission section is made of iron-based material.
- the holding section does not come into direct contact with a sample water, but it has been found that a sample water to which sulfuric acid or the like is added may evaporate and stick to a surface of the holding section, and that iron ions may dissolve into the sample water from that portion.
- the holding section for holding the light emission section of the ultraviolet lamp is formed by a material not including iron. Accordingly, iron ions are not generated even when a reagent that reacts with iron is evaporated and is stuck to the surface of the holding section of the ultraviolet lamp, and interference in the total nitrogen measurement by iron ions may be prevented.
- FIG. 1 is a path diagram schematically showing an embodiment of a total nitrogen measurement apparatus.
- FIG. 2 is a cross-sectional diagram showing an example of a structure of an ultraviolet lamp according to the embodiment.
- FIG. 3 is a flow chart showing a total nitrogen measurement operation of the total nitrogen measurement apparatus according to the embodiment.
- FIG. 4 is measurement data obtained by performing total nitrogen measurement for the same sample for cases where a holding section whose external cylinder portion is made of iron is used in an ultraviolet lamp of an oxidation reactor and where a holding section whose external cylinder portion is made of silicone resin is used in an ultraviolet lamp of an oxidation reactor.
- a holding section for holding a light emission section of an ultraviolet lamp is formed of resin not including a nitrogen component.
- the total nitrogen measurement apparatus includes two multiport valves 10 a and 10 b.
- a sample preparation tank 1 where a sample is prepared and stored is connected to one port of one multiport valve 10 b by a tube 29 .
- a sample inlet/outlet 25 of an oxidation reactor 23 , a measurement section 16 and the like are connected to other ports of the multiport valve 10 b.
- the common port of the multiport valve 10 b is connected to one port of the other multiport valve 10 a.
- Containers 2 to 7 containing various solutions are connected to the ports of the multiport valve 10 a by pipes.
- potassium peroxodisulfate solution is contained in the container 2
- aqueous sodium hydroxide is contained in the container 3
- hydrochloric acid solution is contained in the container 4
- ascorbic acid solution is contained in the container 5
- molybdic acid solution is contained in the container 6
- sulfuric acid solution is contained in the container 7 .
- a syringe pump 17 is connected to the common port of the multiport valve 10 a.
- the syringe pump 17 is driven by a motor 27 , and performs suction and discharge of various liquids.
- the oxidation reactor 23 decomposes nitrogen compounds in a sample into nitrate ions by oxidation.
- the oxidation reactor 23 has a light emission section 30 of an ultraviolet lamp 14 , such as a low pressure mercury lamp, inserted inside a reaction vessel 13 , and is configured to contain a sample water 15 around the ultraviolet lamp 14 .
- the reaction vessel 13 is provided with a heater, and may heat a contained sample to a predetermined temperature.
- the temperature at which the sample water is heated is preferably 100° C. or lower.
- the measurement section 16 measures the absorbance of the sample water after oxidation reaction, and although detailed illustration is omitted, the measurement section 16 is provided with a sample cell, a light source for radiating light of, for example, 220 nm on the sample cell, a sensor for detecting light transmitted through the sample cell, and the like.
- the syringe pump 17 measures a sample water from the sample preparation tank 1 .
- the pure water 9 is suctioned by the syringe pump 17 as necessary, and the sample water is diluted to be, for example, 2 mgN/L or less.
- a solution obtained by adding the potassium peroxodisulfate solution 2 and the sodium hydroxide solution 3 to the sample water is introduced into the reaction vessel 15 of the oxidation reactor 23 heated to about 60 to 80° C.
- ultraviolet rays are radiated by the ultraviolet lamp 14 for about 20 minutes, and nitrogen compounds are decomposed by oxidation into nitrate ions.
- a predetermined amount of solution after the oxidation reaction is measured by the syringe pump 17 , and is transmitted to the measurement section 16 after addition of the hydrochloric acid solution 4 .
- the absorbance at 220 nm is measured at the measurement section 16 , and the total nitrogen concentration is obtained.
- the ultraviolet lamp 14 used by the oxidation reactor 23 will be described with reference to FIG. 2 .
- the ultraviolet lamp 14 includes a light emission section 30 at its tip, and a base portion of the light emission section 30 is held by a holding section 32 .
- the holding section 32 includes, at a tip end of an external cylinder portion 33 , a hole for passing through the light emission section 30 , and a layer 36 formed by solidified filler filled inside the external cylinder portion 33 holds the base portion of the light emission section 30 .
- the external cylinder portion 33 of the holding section 32 is formed of a material other than iron, such as ceramics, alumina, quartz glass, Pyrex (registered trademark) glass, fluoro rubber (for example, Viton (registered trademark)), or tetrafluoroethylene.
- the filler for forming the layer 36 inside the external cylinder portion 33 may be made of low-thermal-expansion silicone resin, epoxy resin, cement, or the like.
- the layer 36 of the filler is formed of silicone resin, and an epoxy resin layer 40 , a silicone resin layer 42 , an epoxy resin layer 44 , and a silicone resin layer 46 are formed, in this order from the silicone resin layer 36 , on the side of the silicone resin layer 36 opposite the light emission section 30 .
- Two lead wires 34 extending from the base portion of the light emission section 30 are drawn outside the holding section 32 by caulking clamps 38 .
- FIG. 4 is measurement data obtained by performing total nitrogen measurement for the same sample for cases where the holding section whose external cylinder portion is made of iron is used in the ultraviolet lamp of the oxidation reactor and where the holding section whose external cylinder portion is made of silicone resin is used in the ultraviolet lamp of the oxidation reactor.
- the nitrogen concentration that is measured is increased with lapse of time.
- the nitrogen concentration that is measured is not changed over time. The reason thereof is assumed to be the dissolution of iron into a reaction solution in the oxidation reactor under an acidic condition by sulfuric acid, the iron which has dissolved into the reaction solution affecting the measurement value of the nitrogen concentration.
- the total nitrogen measurement apparatus of the present embodiment is also capable of decomposing phosphorous compounds into phosphate ions by adding sulfuric acid to a sample water including phosphorous compounds, introducing the sample water into the oxidative decomposition section 23 , and radiating ultraviolet rays at a temperature of 100° C. or lower, and then, of measuring phosphorus concentration by a molybdenum blue method.
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Abstract
Description
- The present invention relates to a total nitrogen measurement apparatus including a reaction vessel having a space where a light emission section of an ultraviolet lamp is to be inserted and where a sample is to be contained in a space around the ultraviolet lamp, the total nitrogen measurement apparatus being for measuring the concentration of nitrogen compounds in a sample by decomposing nitrogen compounds by oxidation by holding, in the reaction vessel, a sample water to which a reactive reagent is added to perform oxidative decomposition of nitrogen compounds and radiating ultraviolet rays from the ultraviolet lamp on the sample water, and performing absorbance measurement on the sample water obtained after the nitrogen compounds have been decomposed by oxidation.
- Generally, as a method of measuring total nitrogen in wastewater discharged from factories and the like, “Ultraviolet spectrophotometry” defined in “Testing methods for industrial wastewater discharged from factories” according to Japanese Industrial Standards is used. This is a method of adding alkaline potassium peroxodisulfate, which is an oxidizing agent, to a sample water, decomposing nitrogen compounds into nitrate ions in a high-temperature and high-pressure environment by thermal decomposition, and determining total nitrogen concentration by absorbance measurement at 220 nm. However, a measurement apparatus to be used for this method has to be resistant to pressure and heat, thus requiring special materials and design.
- As another method of decomposing nitrogen compounds in a sample water into nitrate ions by oxidation, there is an “ultraviolet oxidative decomposition method”. According to this method, total nitrogen concentration is determined by decomposing nitrogen compounds in a sample water to which alkaline potassium peroxodisulfate, which is an oxidizing agent, is added into nitrate ions by oxidation by radiating ultraviolet rays on the sample water under a condition of predetermined temperature and pressure, and measuring the absorbance of the sample water at 220 nm. This method is improved in reducing the pressure and temperature for the sample water, and the temperature necessary for oxidative decomposition of nitrogen oxide by ultraviolet rays is reduced to about 60° C. from conventional 120° C., and also, the pressure may be a normal pressure, and thus, the apparatus is not required to be highly resistant to pressure and heat.
- Patent Document 1: Japanese Patent Laid-open Publication No. 2003-344381
- As an apparatus that uses the ultraviolet oxidative decomposition method, there is an apparatus that adopts a structure according to which, to increase the efficiency of oxidative decomposition of nitrogen compounds, a light emission section of an ultraviolet lamp is inserted inside a reaction vessel of an oxidative decomposition section, and ultraviolet rays are radiated on the nitrogen compounds in a sample water with the light emission section immersed in the sample water (see Patent Document 1). However, a detection signal obtained by performing total nitrogen measurement by an apparatus adopting such a structure sometimes includes a signal which is thought to be caused by the influence of a substance different from the nitrate ions generated by oxidative decomposition of the nitrogen compounds, and the cause of the obtained detection signal is yet to be explained.
- Accordingly, the present invention aims to prevent, in measurement of absorbance of a sample water including nitrate ions which have been converted by ultraviolet radiation, interference in total nitrogen measurement by substances other than the nitrate ions.
- The present invention is a total nitrogen measurement apparatus including a reaction vessel having a space where a light emission section of an ultraviolet lamp is to be inserted and where a sample is to be contained in a space around the ultraviolet lamp, the total nitrogen measurement apparatus being for measuring a total nitrogen concentration of a sample water by converting nitrogen compounds into nitrate ions by oxidative decomposition by holding, in the reaction vessel, a sample to which a reactive reagent is added to perform oxidative decomposition of the nitrogen compounds and radiating ultraviolet rays from the ultraviolet lamp on the sample water, and performing absorbance measurement on the sample water including the nitrate ions, wherein a holding section for holding the light emission section of the ultraviolet lamp is formed of a material not including iron.
- In the case of performing total nitrogen measurement by measuring the absorbance around 220 nm, measurement is affected by substances having absorption in a wavelength range around 220 nm. Among such substances, an iron ion greatly interferes with total nitrogen measurement, and thus, a structure is adopted according to which a member formed of an iron-based material does not come into contact with a sample water. Nevertheless, a noise presumably caused by a component different from the nitrate ion is included in a detection signal.
- The present inventors have found out that the cause of the noise is the ultraviolet lamp which is for radiating ultraviolet rays on the sample water to decompose the nitrogen compounds by oxidation. That is, although the only part of the ultraviolet lamp that comes into contact with a sample water is a light emission section formed of a material not including iron-based material, such as a quartz glass tube, an external cylinder portion of a holding section for holding the base portion of the light emission section is made of iron-based material. The holding section does not come into direct contact with a sample water, but it has been found that a sample water to which sulfuric acid or the like is added may evaporate and stick to a surface of the holding section, and that iron ions may dissolve into the sample water from that portion.
- Based on the above understanding, according to the present invention, the holding section for holding the light emission section of the ultraviolet lamp is formed by a material not including iron. Accordingly, iron ions are not generated even when a reagent that reacts with iron is evaporated and is stuck to the surface of the holding section of the ultraviolet lamp, and interference in the total nitrogen measurement by iron ions may be prevented.
-
FIG. 1 is a path diagram schematically showing an embodiment of a total nitrogen measurement apparatus. -
FIG. 2 is a cross-sectional diagram showing an example of a structure of an ultraviolet lamp according to the embodiment. -
FIG. 3 is a flow chart showing a total nitrogen measurement operation of the total nitrogen measurement apparatus according to the embodiment. -
FIG. 4 is measurement data obtained by performing total nitrogen measurement for the same sample for cases where a holding section whose external cylinder portion is made of iron is used in an ultraviolet lamp of an oxidation reactor and where a holding section whose external cylinder portion is made of silicone resin is used in an ultraviolet lamp of an oxidation reactor. - 1: Sample preparation tank
- 2 to 9: Reagent containers
- 10 a, 10 b: Multiport valve
- 13: Reaction vessel
- 14: Ultraviolet lamp
- 15: Sample water
- 16: Measurement section
- 23: Oxidation reactor
- 30: Light emission section
- 32: Holding section
- 34: Lead wire
- 36: Filler
- According to a preferred embodiment of a total nitrogen measurement apparatus of the present invention, a holding section for holding a light emission section of an ultraviolet lamp is formed of resin not including a nitrogen component.
- In the following, an embodiment of the total nitrogen measurement apparatus will be described with reference to
FIG. 1 . The total nitrogen measurement apparatus includes twomultiport valves sample preparation tank 1 where a sample is prepared and stored is connected to one port of onemultiport valve 10 b by atube 29. In addition to acontainer 8 containing span solution and acontainer 9 containing pure water, a sample inlet/outlet 25 of anoxidation reactor 23, ameasurement section 16 and the like are connected to other ports of themultiport valve 10 b. Also, the common port of themultiport valve 10 b is connected to one port of theother multiport valve 10 a. -
Containers 2 to 7 containing various solutions are connected to the ports of themultiport valve 10 a by pipes. In the present embodiment, potassium peroxodisulfate solution is contained in thecontainer 2, aqueous sodium hydroxide is contained in thecontainer 3, hydrochloric acid solution is contained in thecontainer 4, ascorbic acid solution is contained in thecontainer 5, molybdic acid solution is contained in thecontainer 6, and sulfuric acid solution is contained in thecontainer 7. - A
syringe pump 17 is connected to the common port of themultiport valve 10 a. Thesyringe pump 17 is driven by amotor 27, and performs suction and discharge of various liquids. - The
oxidation reactor 23 decomposes nitrogen compounds in a sample into nitrate ions by oxidation. Theoxidation reactor 23 has alight emission section 30 of anultraviolet lamp 14, such as a low pressure mercury lamp, inserted inside areaction vessel 13, and is configured to contain asample water 15 around theultraviolet lamp 14. Although not shown, thereaction vessel 13 is provided with a heater, and may heat a contained sample to a predetermined temperature. The temperature at which the sample water is heated is preferably 100° C. or lower. - The
measurement section 16 measures the absorbance of the sample water after oxidation reaction, and although detailed illustration is omitted, themeasurement section 16 is provided with a sample cell, a light source for radiating light of, for example, 220 nm on the sample cell, a sensor for detecting light transmitted through the sample cell, and the like. - Next, a measurement operation of the total nitrogen measurement apparatus will be described with reference to the flow chart of
FIG. 3 . - The
syringe pump 17 measures a sample water from thesample preparation tank 1. Thepure water 9 is suctioned by thesyringe pump 17 as necessary, and the sample water is diluted to be, for example, 2 mgN/L or less. - A solution obtained by adding the
potassium peroxodisulfate solution 2 and thesodium hydroxide solution 3 to the sample water is introduced into thereaction vessel 15 of theoxidation reactor 23 heated to about 60 to 80° C. At theoxidation reactor 23, ultraviolet rays are radiated by theultraviolet lamp 14 for about 20 minutes, and nitrogen compounds are decomposed by oxidation into nitrate ions. Subsequently, a predetermined amount of solution after the oxidation reaction is measured by thesyringe pump 17, and is transmitted to themeasurement section 16 after addition of thehydrochloric acid solution 4. Then, the absorbance at 220 nm is measured at themeasurement section 16, and the total nitrogen concentration is obtained. - Here, the
ultraviolet lamp 14 used by theoxidation reactor 23 will be described with reference toFIG. 2 . - The
ultraviolet lamp 14 includes alight emission section 30 at its tip, and a base portion of thelight emission section 30 is held by a holdingsection 32. The holdingsection 32 includes, at a tip end of anexternal cylinder portion 33, a hole for passing through thelight emission section 30, and alayer 36 formed by solidified filler filled inside theexternal cylinder portion 33 holds the base portion of thelight emission section 30. Theexternal cylinder portion 33 of the holdingsection 32 is formed of a material other than iron, such as ceramics, alumina, quartz glass, Pyrex (registered trademark) glass, fluoro rubber (for example, Viton (registered trademark)), or tetrafluoroethylene. When these materials are used for theexternal cylinder portion 33, the filler for forming thelayer 36 inside theexternal cylinder portion 33 may be made of low-thermal-expansion silicone resin, epoxy resin, cement, or the like. In the present embodiment, thelayer 36 of the filler is formed of silicone resin, and anepoxy resin layer 40, asilicone resin layer 42, anepoxy resin layer 44, and asilicone resin layer 46 are formed, in this order from thesilicone resin layer 36, on the side of thesilicone resin layer 36 opposite thelight emission section 30. Twolead wires 34 extending from the base portion of thelight emission section 30 are drawn outside the holdingsection 32 by caulking clamps 38. - At the
oxidation reactor 23, only thelight emission section 30 of theultraviolet lamp 14 is inserted inside thereaction vessel 13, and the sample water is contained around thislight emission section 30. Potassium peroxodisulfate and sodium hydroxide are added to the sample water to be contained, and these liquids may evaporate and stick to the external cylinder portion of the holdingsection 32 of theultraviolet lamp 14, but since the external cylinder portion of the holdingsection 32 is made of a material other than iron, iron ions that have absorption with respect to light at 220 nm are not generated, and measurement of ultraviolet absorbance is not affected. -
FIG. 4 is measurement data obtained by performing total nitrogen measurement for the same sample for cases where the holding section whose external cylinder portion is made of iron is used in the ultraviolet lamp of the oxidation reactor and where the holding section whose external cylinder portion is made of silicone resin is used in the ultraviolet lamp of the oxidation reactor. As indicated by this data, in the case where the external cylinder portion of the holding section of the ultraviolet lamp is made of iron, the nitrogen concentration that is measured is increased with lapse of time. On the other hand, in the case where the external cylinder portion of the holding section of the ultraviolet lamp is made of silicone resin, the nitrogen concentration that is measured is not changed over time. The reason thereof is assumed to be the dissolution of iron into a reaction solution in the oxidation reactor under an acidic condition by sulfuric acid, the iron which has dissolved into the reaction solution affecting the measurement value of the nitrogen concentration. - Additionally, the total nitrogen measurement apparatus of the present embodiment is also capable of decomposing phosphorous compounds into phosphate ions by adding sulfuric acid to a sample water including phosphorous compounds, introducing the sample water into the
oxidative decomposition section 23, and radiating ultraviolet rays at a temperature of 100° C. or lower, and then, of measuring phosphorus concentration by a molybdenum blue method.
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PCT/JP2012/053790 WO2013121577A1 (en) | 2012-02-17 | 2012-02-17 | Total nitrogen measurement apparatus |
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JP (1) | JP5854122B2 (en) |
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CN108507960A (en) * | 2017-02-27 | 2018-09-07 | 北新集团建材股份有限公司 | The quantitative analysis method of total nitrogen and nitrate nitrogen in desulfurated plaster |
US10955341B2 (en) | 2016-03-09 | 2021-03-23 | Ysi, Inc. | Optical nitrate sensor compensation algorithm for multiparameter water quality measurement |
US11073475B2 (en) | 2016-03-07 | 2021-07-27 | Ysi, Inc. | Optical nitrate sensor for multiparameter water quality measurement |
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JP6167967B2 (en) * | 2014-03-31 | 2017-07-26 | 株式会社島津製作所 | Ultraviolet irradiation device and analyzer equipped with the same |
CN104792704B (en) * | 2015-03-31 | 2017-04-05 | 烟台大学 | Tri- index continuous synchronization real-time online determining instrument of TOC, TN, TP |
CN104730266B (en) * | 2015-03-31 | 2016-07-20 | 烟台大学 | The method of a kind of total organic carbon continuous the real time measure Tong Bu with total nitrogen and instrument |
CN115917294A (en) * | 2020-06-12 | 2023-04-04 | 株式会社岛津制作所 | Water quality analyzer and water quality analyzing method |
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EP0531625B1 (en) * | 1991-05-30 | 1997-08-20 | Canon Kabushiki Kaisha | Light-receiving member |
JP3237400B2 (en) | 1994-05-16 | 2001-12-10 | 株式会社島津製作所 | Analyzer for nitrogen compounds and phosphorus compounds in water |
JP3269196B2 (en) | 1993-07-14 | 2002-03-25 | 株式会社島津製作所 | Analyzer for nitrogen compounds and phosphorus compounds in water |
US5567621A (en) | 1993-07-14 | 1996-10-22 | Shimadzu Corporation | Method of and apparatus for analyzing nitrogen compound and phosphorus compound contained in water |
JPH09281099A (en) | 1996-04-12 | 1997-10-31 | Akira Fujishima | Method and apparatus for analyzing underwater compound |
JP2001056332A (en) | 1999-08-20 | 2001-02-27 | Shimadzu Corp | Water analyzer |
JP2001083083A (en) | 1999-09-14 | 2001-03-30 | Dkk Toa Corp | Method and device for measuring total nitrogen |
JP2001194357A (en) | 2000-01-07 | 2001-07-19 | Meidensha Corp | Total nitrogen concentration measuring method, and its apparatus |
JP4045859B2 (en) | 2002-05-24 | 2008-02-13 | 株式会社島津製作所 | Total nitrogen measurement method |
CN2555504Y (en) | 2002-08-12 | 2003-06-11 | 广州市怡文科技有限公司 | Total phosphorous on-line automatic monitor for water quality |
CN1506672A (en) | 2002-12-10 | 2004-06-23 | 天津大学 | Ultraviolet oxidation process and device for intermittent in-situ quick resolution of total phosphorus and total nitrogen |
JP4661232B2 (en) | 2005-01-24 | 2011-03-30 | 株式会社島津製作所 | Total nitrogen measuring method and apparatus |
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Cited By (3)
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US11073475B2 (en) | 2016-03-07 | 2021-07-27 | Ysi, Inc. | Optical nitrate sensor for multiparameter water quality measurement |
US10955341B2 (en) | 2016-03-09 | 2021-03-23 | Ysi, Inc. | Optical nitrate sensor compensation algorithm for multiparameter water quality measurement |
CN108507960A (en) * | 2017-02-27 | 2018-09-07 | 北新集团建材股份有限公司 | The quantitative analysis method of total nitrogen and nitrate nitrogen in desulfurated plaster |
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CN104115009A (en) | 2014-10-22 |
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